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rs151340624

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151340624(C;T)
Make rs151340624(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50090846
GeneCLCN5
is asnp
is mentioned by
dbSNPrs151340624
ebirs151340624
HLIrs151340624
Exacrs151340624
Varsomers151340624
Maprs151340624
PheGenIrs151340624
hapmaprs151340624
1000 genomesrs151340624
hgdprs151340624
ensemblrs151340624
gopubmedrs151340624
geneviewrs151340624
scholarrs151340624
googlers151340624
pharmgkbrs151340624
gwascentralrs151340624
openSNPrs151340624
23andMers151340624
23andMe allrs151340624
SNP Nexus

SNPshotrs151340624
SNPdbers151340624
MSV3drs151340624
GWAS Ctlgrs151340624
Max Magnitude0
ClinVar
Risk rs151340624(T;T)
Alt rs151340624(T;T)
Reference rs151340624(C;C)
Significance Pathogenic
Disease Nephrolithiasis
Variation info
Gene CLCN5
CLNDBN Nephrolithiasis, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.49855503C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012568.14,